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无低丙种球蛋白血症或吸收不良综合征的大肠弥漫性结节性淋巴组织增生:1例报告及文献复习

Diffuse nodular lymphoid hyperplasia of the large bowel without hypogammaglobulinemia or malabsorption syndrome: a case report and literature review.

作者信息

Tomita Shigeki, Kojima Masaru, Imura Johji, Ueda Yoshihiko, Koitabashi Ayako, Suzuki Yasunaga, Nakamura Yuichi, Mitani Kinuko, Terano Akira, Fujimori Takahiro

机构信息

Department of Surgical and Molecular Pathology, Dokkyo University School of Medicine, Mibu, Tochigi, Japan.

出版信息

Int J Surg Pathol. 2002 Oct;10(4):297-302. doi: 10.1177/106689690201000411.

Abstract

Diffuse nodular lymphoid hyperplasia (DNLH) of the intestine is an extremely rare lymphoproliferative disorder occasionally associated with non-Hodgkin lymphomas. We report an unusual case of DNLH of the entire colon, which resembled malignant lymphoma (particularly low-grade B-cell lymphoma) both on clinical and pathologic grounds. The patient was a 62-year-old Japanese woman who was found to have multiple polypoid lesions along the entire large intestine by colonoscopy. Abdominal computed tomography revealed hepatosplenomegaly and multiple mesenteric lymphadenopathy. Histologically, the lesion was characterized by numerous lymphoid follicles with active germinal centers and a diffuse infiltrate of lymphoid cells in the mucosa and submucosa. The present case appears to be an essentially benign condition bearing a resemblance, both clinically and histologically, to malignant lymphoma, and from which it can be distinguished by use of immunohistochemical or molecular analysis.

摘要

肠道弥漫性结节性淋巴组织增生(DNLH)是一种极为罕见的淋巴增殖性疾病,偶尔与非霍奇金淋巴瘤相关。我们报告一例全结肠DNLH的罕见病例,该病例在临床和病理方面均类似于恶性淋巴瘤(尤其是低度B细胞淋巴瘤)。患者为一名62岁的日本女性,结肠镜检查发现整个大肠有多个息肉样病变。腹部计算机断层扫描显示肝脾肿大和多处肠系膜淋巴结病。组织学上,病变的特征是有许多具有活跃生发中心的淋巴滤泡,以及黏膜和黏膜下层淋巴细胞的弥漫性浸润。本病例似乎本质上是一种良性疾病,在临床和组织学上与恶性淋巴瘤相似,可通过免疫组织化学或分子分析与之鉴别。

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